Distribution and Autecology of Chrysophyte Cysts from High Arctic Svalbard Lakes: Preliminary Evidence of Recent Environmental Change

Chrysophycean stomatocyst assemblages were analysed from the sediments of 17 lakes and ponds from Svalbard as one component of a multi-proxy investigation of recent environmental change in the high Arctic. Sediment cores and water chemistry were collected from each of the study lakes, and chrysophyte stomatocysts were investigated from the top 0.25 cm of sediment (present-day) and bottom (i.e., bottom of short sediment core, pre-industrial) sediment samples. This study represents the first undertaking of chrysophyte cyst morphology and distribution on Svalbard. A total of 153 cyst morphotypes were described with light microscopy and/or scanning electron microscopy, of which 21 are new forms. Canonical correspondence analysis indicates that the present-day distribution of cysts is significantly related to pH (p= 0.02), altitude (p= 0.02), and Na⁺ (p= 0.04). Marked shifts in chrysophyte cyst assemblages were recorded between the top and bottom sediment samples of most lakes. A recent study has demonstrated that Svalbard lakes receive atmospheric contaminants from both local and remote sources. The observed assemblage shifts may be the result of the combined effects of these point sources and long-range pollutants, or the effects of recent climate change, or both.     

29Si and 1H NMR spectroscopy of high-pressure hydrous magnesium silicates

We present NMR spectroscopic data, obtained by ¹H MAS, ¹H static spin-echo, and ²⁹Si{¹H} CP-MAS techniques, for a series of hydrous magnesium silicate samples synthesized at high pressure. This series includes chondrodite, β-Mg₂SiO₄, and phases A, B, superhydrous B, and E. Phases B and superhydrous B give very narrow ²⁹Si NMR peaks and display the most de-shielded Si^VI chemical shifts yet reported: ?170.4?ppm for B and ?166.6 for superhydrous B. The ¹H NMR spectra of B and superhydrous B confirm the presence of paired hydroxyls, as determined from refinement of the H positions from X-ray diffraction data. The ¹H MAS NMR spectra of phase B contain peaks for the two distinct hydrogen positions, with chemical shifts of +4.7 and +3.3?ppm. The static ¹H spectrum contains a powder pattern characteristic of a strongly coupled hydrogen pair, from which a dipolar coupling constant of 18.6(4)?kHz and inter-hydrogen distance of d(H–H)=1.86(2)?Å were obtained. Superhydrous B appears to give two poorly resolved ¹H MAS peaks, consistent with the presence of two distinct hydrogen pairs in the P2₁ mn crystal structure. Analysis of its spin-echo spectrum gives d(H–H)=1.83(3)?Å, slightly shorter than for phase B. β-Mg₂SiO₄, coexisting with phases B and superhydrous B, appears to give ²⁹Si{¹H} CP-MAS signal, indicating that it contains significant H concentration. The ²⁹Si chemical shifts for phases B, superhydrous B, and chondrodite, together with those reported previously for other Mg-silicates, show a good correlation with structural parameters.     

Thermodynamic data of lawsonite and zoisite in the system CaO–Al2O3–SiO2–H2O based on experimental phase equilibria and calorimetric work

The enthalpy of drop-solution in molten 2PbO·B₂O₃ of synthetic and natural lawsonite, CaAl₂(Si₂O₇)(OH)₂·H₂O, was measured by high-temperature oxide melt calorimetry. The enthalpy of formation determined for the synthetic material is (_fH^Oxides=-168.7Dž.4 kJ mol^-1, or (_fH⁰₂₉₈=-4,872.5dž.0 kJ mol^-1. These values are in reasonable agreement with previously published data, although previous calorimetric work yielded slightly more exothermic data and optimisation methods resulted in slightly less exothermic values. The equilibrium conditions for the dehydration of lawsonite to zoisite, kyanite and quartz/coesite at pressures and temperatures up to 5 GPa and 850 °C were determined by piston cylinder experiments. These results, other recent phase equilibrium data, and new calorimetric and thermophysical data for lawsonite and zoisite, Ca₂Al₃(SiO₄)(Si₂O₇)O(OH), were used to constrain a mathematical programming analysis of the thermodynamic data for these two minerals in the chemical system CaO-Al₂O₃-SiO₂-H₂O (CASH). The following data for lawsonite and zoisite were obtained: (_fH⁰₂₉₈ (lawsonite)=-4,865.68 kJ mol^-1 , S⁰₂₉₈ (lawsonite)=229.27 J K^-1 mol^-1 , (_fH⁰₂₉₈ (zoisite)=-6,888.99 kJ mol^-1 , S⁰₂₉₈ (zoisite)=297.71 J K^-1 mol^-1 . Additionally, a recalculation of the bulk modulus of lawsonite yielded K=120.7 GPa, which is in good agreement with recent experimental work.     

Calorimetric study of high-pressure polymorphs of MnSiO3

With increasing pressure, MnSiO₃ rhodonite stable at atmospheric pressure transforms to pyroxmangite, then to clinopyroxene and further to tetragonal garnet, which finally decomposes into MnO (rocksalt) plus SiO₂ (stishovite). High temperature solution calorimetry of synthetic rhodonite, clinopyroxene and garnet forms of MnSiO₃ was used to measure the enthalpies of these transitions. ΔH ₉₇₄ ⁰ for the rhodonite-clinopyroxene and ΔH ₂₉₈ ⁰ for the clinopyroxene-garnet transition are 520±490 and 8,270±590 cal/mol, respectively. The published data on the enthalpy of the rhodonite-pyroxmangite transition, phase equilibrium boundaries, compressibility and thermal expansion data are used to calculate entropy changes for the transitions. The enthalpy, entropy and volume changes are very small for all the transitions among rhodonite, pyroxmangite and clinopyroxene. The calculated boundary for the clinopyroxene-garnet transition is consistent with the published experimental results. The pyroxene-garnet transition in several materials, including MnSiO₃, is characterized by a relatively small negative entropy change and large volume decrease, resulting in a small positiveP – T slope. The disproportionation of MnSiO₃ garnet to MnO plus stishovite and of Mn₂SiO₄ olivine to garnet plus MnO are calculated to occur at about 17–18 and 14–15 GPa, respectively, at 1,000–1,500 K.     

Enthalpy effects associated with Al/Si ordering in anhydrous Mg-cordierite

Measurements of the heats of solution (ΔH_soln) in molten Pb₂B₂O₅ at 708°C of anhydrous magnesian cordierites, prepared with a range of structural states, show that the enthalpy effect associated with Al/Si ordering is substantial (? 9.76 ± 1.56 kcal mole^?1). Differences in the state of order between synthetic cordierites used in phase equilibrium studies and cordierites in the natural environment could lead to significant errors in the estimation of palaeo-pressures and temperatures. A continuous change of ΔH_soln with annealing time supports the suggestion of putnis (1980) that the hexagonal → orthorhombic transformation in cordierite, which can occur via a modulated structure, is truly continuous under metastable conditions. In addition, a linear relation between ΔH_soln and the logarithm of annealing time has been found, which provides some insight into the nature of the ordering mechanisms at an atomic level. Al and Si exchanges occur continuously between neighbouring tetrahedral sites with a net drift towards increasing order. No kinetic or thermochemical distinction can be made between the development of long range and short range order.The enthalpy of vitrification (~ 12 kcal mole^?1) for a metastable stuffed β-quartz polymorph of cordierite composition is similar to that for pure quartz (on a per two oxygen basis), while the heat of vitrification for even the most disordered cordierite seen in this study is more than a factor of three greater (~40 kcal mole^?1). This is consistent with the view that cordierite glass resembles the quartz structure more closely than the crystalline cordierite structure, and that crystallisation of the glass below ~900°C is controlled by a tetrahedral framework.     

New data on the palaeobiogeography of Loftusia genus (Foraminiferida). An in situ presence of the genus in eastern Greece (Boeotia)

An Upper Maastrichtian horizon rich in Loftusia is for the first time described in situ in Greece in the province of Boeotia. It is found in a continuous undisturbed carbonate sequence of the eastern Greece platform (Subpelagonian zone) of Maastrichtian–Paleocene age followed by flysch sedimentation. Loftusia is found in a facies reflecting an outer shelf environment, associated with debris of rudists, Orbitoides spp., Siderolites calcitrapoides, Omphalocyclus macroporus, Hellenocyclina beotica, Sulcoperculina sp., and echinoderms. Similar fauna, but without Loftusia, is found in the surrounding levels of Late Maastrichtian age as well. This recovery of the genus in the western part of its distribution area, where it is not as abundant as in the eastern part, is considered significant for the palaeobiogeography of the genus in Tethys Ocean during Late Cretaceous. To cite this article: A. Zambetakis-Lekkas, A. Kemeridou, C. R. Geoscience 338 (2006).     

Combining geographic information system, multicriteria evaluation techniques and fuzzy logic in siting MSW landfills

This study presents a methodology for siting municipal solid waste landfills, coupling geographic information systems (GIS), fuzzy logic, and multicriteria evaluation techniques. Both exclusionary and non-exclusionary criteria are used. Factors, i.e., non-exclusionary criteria, are divided in two distinct groups which do not have the same level of trade off. The first group comprises factors related to the physical environment, which cannot be expressed in terms of monetary cost and, therefore, they do not easily trade off. The second group includes those factors related to human activities, i.e., socioeconomic factors, which can be expressed as financial cost, thus showing a high level of trade off. GIS are used for geographic data acquisition and processing. The analytical hierarchy process (AHP) is the multicriteria evaluation technique used, enhanced with fuzzy factor standardization. Besides assigning weights to factors through the AHP, control over the level of risk and trade off in the siting process is achieved through a second set of weights, i.e., order weights, applied to factors in each factor group, on a pixel-by-pixel basis, thus taking into account the local site characteristics. The method has been applied to Evros prefecture (NE Greece), an area of approximately 4,000 km². The siting methodology results in two intermediate suitability maps, one related to environmental and the other to socioeconomic criteria. Combination of the two intermediate maps results in the final composite suitability map for landfill siting.     

Respiration and denitrification in permeable continental shelf deposits on the South Atlantic Bight: Rates of carbon and nitrogen cycling from sediment column experiments

Nitrogen (N) cycling and respiration rates were measured in sediment columns packed with southeastern United States continental shelf sands, with high permeability (4.66×10⁻¹¹ m²) and low organic carbon (0.05%) and nitrogen (0.008%). To simulate porewater advection, natural shelf seawater was pumped through columns of different lengths to achieve fluid residence times of approximately 3, 6, and 12 h. Experiments were conducted seasonally at in situ temperature. Fluid flow was uniform in nearly all columns, with minimal dead zones and channeling. Significant respiration (O₂ consumption and ∑CO₂ production) occurred in all columns, with highest respiration rates in summer. Most (78–100%) remineralized N was released as N₂ in the majority of cases, including columns with oxic porewater throughout, with only a small fraction released as NO₃⁻ from some oxic columns. A rate of 0.84–4.83×10¹⁰ mol N yr⁻¹, equivalent to 1.06–6.09×10⁻⁶ mmol N cm⁻² h⁻¹, was calculated for benthic N₂ production in the South Atlantic Bight, which can account for a large fraction of new N inputs to this shelf region. Metal and sulfate reduction occurred in long residence time columns with anoxic outflow in summer and fall, when respiration rates were highest. Because permeable sediments dominate continental shelves, N₂ production in high permeability coastal sediments may play an important role in the global N cycle.     

The sinking of Mexico City: Its effects on soil properties and seismic response

Extensive pumping to extract water from Mexico City's subsoil has caused regional sinking. Water pumping produces regional consolidation which increases effective stresses acting on the subsoil modifying its static and dynamic properties. As the soil properties change, so does their dynamic response. Approximate expressions to estimate the future changes in soil properties are proposed. Also, this paper puts forth new evidence to illustrate these changes and presents estimates of future settlements in central Mexico City, using a soil consolidation model that overcomes some of the limitations of Terzaghi's theory. Results of an analysis to estimate the effects of the evolution of the subsoil's dynamic properties are illustrated by means of seismic analyses performed on a couple of sites in an old lake bed in Mexico City.     

Achievability of the Paris Agreement targets in the EU: demand-side reduction potentials in a carbon budget perspective

Limiting global warming to ‘well below’ 2°C above pre-industrial levels and pursuing efforts to limit the temperature increase even further to 1.5°C is an integral part of the 2015 Paris Agreement. To achieve these aims, cumulative global carbon emissions after 2016 should not exceed 940 – 390?Gt of CO₂ (for the 2°C target) and 167 – ?48?Gt of CO₂ (for the 1.5°C target) by the end of the century. This paper analyses the EU’s cumulative carbon emissions in different models and scenarios (global models, EU-focused models and national carbon mitigation scenarios). Due to the higher reductions in energy use and carbon intensity of the end-use sectors in the national scenarios, we identify an additional mitigation potential of 26–37 Gt cumulative CO₂ emissions up to 2050 compared to what is currently included in global or EU scenarios. These additional reductions could help to both reduce the need for carbon dioxide removals and bring cumulative emissions in global and EU scenarios in line with a fairness-based domestic EU budget for a 2°C target, while still remaining way above the budget for 1.5°C.

Key policy insights

• Models used for policy advice such as global integrated assessment models or EU models fail to consider certain mitigation potential available at the level of sectors.

• Global and EU models assume significant levels of CO₂ emission reductions from carbon capture and storage to reach the 1.5°C target but also to reach the 2°C target.

• Global and EU model scenarios are not compatible with a fair domestic EU share in the global carbon budget either for 2°C or for 1.5°C.

• Integrating additional sectoral mitigation potential from detailed national models can help bring down cumulative emissions in global and EU models to a level comparable to a fairness-based domestic EU share compatible with the 2°C target, but not the 1.5°C aspiration.